Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.
Identifieur interne : 001B60 ( PubMed/Curation ); précédent : 001B59; suivant : 001B61Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.
Auteurs : Juan M. Politei [Argentine] ; Didier Bouhassira [France] ; Dominique P. Germain [France] ; Cyril Goizet [France] ; Antonio Guerrero-Sola [Espagne] ; Max J. Hilz [Allemagne] ; Elspeth J. Hutton [Australie] ; Amel Karaa [États-Unis] ; Rocco Liguori [Italie] ; Nurcan Üçeyler [Allemagne] ; Lonnie K. Zeltzer [États-Unis] ; Alessandro Burlina [Italie]Source :
- CNS neuroscience & therapeutics [ 1755-5949 ] ; 2016.
Descripteurs français
- KwdFr :
- Analgésiques non narcotiques (usage thérapeutique), Anti-inflammatoires non stéroïdiens (usage thérapeutique), Diagnostic différentiel, Douleur (diagnostic), Douleur (étiologie), Enquêtes et questionnaires, Femelle, Ganglions sensitifs des nerfs spinaux (anatomopathologie), Gestion de la douleur (), Humains, Maladie de Fabry (), Maladie de Fabry (anatomopathologie), Mesure de la douleur, Mode de vie, Mâle, Thérapie enzymatique substitutive.
- MESH :
- anatomopathologie : Ganglions sensitifs des nerfs spinaux, Maladie de Fabry.
- diagnostic : Douleur.
- usage thérapeutique : Analgésiques non narcotiques, Anti-inflammatoires non stéroïdiens.
- étiologie : Douleur.
- Diagnostic différentiel, Enquêtes et questionnaires, Femelle, Gestion de la douleur, Humains, Maladie de Fabry, Mesure de la douleur, Mode de vie, Mâle, Thérapie enzymatique substitutive.
English descriptors
- KwdEn :
- Analgesics, Non-Narcotic (therapeutic use), Anti-Inflammatory Agents, Non-Steroidal (therapeutic use), Diagnosis, Differential, Enzyme Replacement Therapy, Fabry Disease (complications), Fabry Disease (pathology), Fabry Disease (therapy), Female, Ganglia, Spinal (pathology), Humans, Life Style, Male, Pain (diagnosis), Pain (etiology), Pain Management (methods), Pain Measurement, Surveys and Questionnaires.
- MESH :
- chemical , therapeutic use : Analgesics, Non-Narcotic, Anti-Inflammatory Agents, Non-Steroidal.
- complications : Fabry Disease.
- diagnosis : Pain.
- etiology : Pain.
- methods : Pain Management.
- pathology : Fabry Disease, Ganglia, Spinal.
- therapy : Fabry Disease.
- Diagnosis, Differential, Enzyme Replacement Therapy, Female, Humans, Life Style, Male, Pain Measurement, Surveys and Questionnaires.
Abstract
Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.
DOI: 10.1111/cns.12542
PubMed: 27297686
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pubmed:27297686Le document en format XML
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<term>Enzyme Replacement Therapy</term>
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<term>Douleur (étiologie)</term>
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<term>Maladie de Fabry (anatomopathologie)</term>
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<term>Mode de vie</term>
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<term>Enzyme Replacement Therapy</term>
<term>Female</term>
<term>Humans</term>
<term>Life Style</term>
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<term>Pain Measurement</term>
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<term>Enquêtes et questionnaires</term>
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<front><div type="abstract" xml:lang="en">Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.</div>
</front>
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<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">27297686</PMID>
<DateCreated><Year>2016</Year>
<Month>06</Month>
<Day>14</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>04</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised><Year>2017</Year>
<Month>04</Month>
<Day>17</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1755-5949</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>22</Volume>
<Issue>7</Issue>
<PubDate><Year>2016</Year>
<Month>07</Month>
</PubDate>
</JournalIssue>
<Title>CNS neuroscience & therapeutics</Title>
<ISOAbbreviation>CNS Neurosci Ther</ISOAbbreviation>
</Journal>
<ArticleTitle>Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.</ArticleTitle>
<Pagination><MedlinePgn>568-76</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/cns.12542</ELocationID>
<Abstract><AbstractText Label="AIMS">Patients with Fabry disease (FD) characteristically develop peripheral neuropathy at an early age, with pain being a crucial symptom of underlying pathology. However, the diagnosis of pain is challenging due to the heterogeneous and nonspecific symptoms. Practical guidance on the diagnosis and management of pain in FD is needed.</AbstractText>
<AbstractText Label="METHODS">In 2014, experts met to discuss recent advances on this topic and update clinical guidance.</AbstractText>
<AbstractText Label="RESULTS">Emerging disease-specific tools, including FabryScan, Fabry-specific Pediatric Health and Pain Questionnaire, and Würzburg Fabry Pain Questionnaire, and more general tools like the Total Symptom Score can aid diagnosis, characterization, and monitoring of pain in patients with FD. These tools can be complemented by more objective and quantifiable sensory testing. In male and female patients of any age, pain related to FD can be an early indication to start disease-specific enzyme replacement therapy before potentially irreversible organ damage to the kidneys, heart, or brain occurs.</AbstractText>
<AbstractText Label="CONCLUSION">To improve treatment outcomes, pain should be diagnosed early in unrecognized or newly identified FD patients. Treatment should include: (a) enzyme replacement therapy controlling the progression of underlying pathology; (b) adjunctive, symptomatic pain management with analgesics for chronic neuropathic and acute nociceptive, and inflammatory or mixed pain; and (c) lifestyle modifications.</AbstractText>
<CopyrightInformation>© 2016 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Politei</LastName>
<ForeName>Juan M</ForeName>
<Initials>JM</Initials>
<AffiliationInfo><Affiliation>Fundación para el Estudio de las Enfermedades Neurometabólicas (FESEN), Buenos Aires, Argentina.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bouhassira</LastName>
<ForeName>Didier</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>INSERM U-987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Germain</LastName>
<ForeName>Dominique P</ForeName>
<Initials>DP</Initials>
<AffiliationInfo><Affiliation>Division of Medical Genetics, University of Versailles - St Quentin en Yvelines, Paris-Saclay University, Montigny, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Goizet</LastName>
<ForeName>Cyril</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>CHU Bordeaux, Hôpital Pellegrin, Service de Génétique Médicale and Université Bordeaux, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM) EA4576, Bordeaux, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Guerrero-Sola</LastName>
<ForeName>Antonio</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Neuromuscular Unit, Neurology Department, Hospital Clínico San Carlos, Madrid, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hilz</LastName>
<ForeName>Max J</ForeName>
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<Initials>EJ</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, The Alfred Hospital, Melbourne, Vic., Australia.</Affiliation>
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<Initials>A</Initials>
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<MeshHeadingList><MeshHeading><DescriptorName UI="D018712" MajorTopicYN="N">Analgesics, Non-Narcotic</DescriptorName>
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<MeshHeading><DescriptorName UI="D005727" MajorTopicYN="N">Ganglia, Spinal</DescriptorName>
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<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
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<MeshHeading><DescriptorName UI="D010146" MajorTopicYN="N">Pain</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName>
<QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Diagnosis</Keyword>
<Keyword MajorTopicYN="Y">Enzyme replacement therapy</Keyword>
<Keyword MajorTopicYN="Y">Fabry disease</Keyword>
<Keyword MajorTopicYN="Y">Pain</Keyword>
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<Day>26</Day>
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